TWI599604B - Modified polymer materials and composite stabilizer composition - Google Patents
Modified polymer materials and composite stabilizer composition Download PDFInfo
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- TWI599604B TWI599604B TW105126497A TW105126497A TWI599604B TW I599604 B TWI599604 B TW I599604B TW 105126497 A TW105126497 A TW 105126497A TW 105126497 A TW105126497 A TW 105126497A TW I599604 B TWI599604 B TW I599604B
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- 239000000203 mixture Substances 0.000 title claims description 23
- 239000002861 polymer material Substances 0.000 title claims description 16
- 239000006084 composite stabilizer Substances 0.000 title claims description 15
- 239000000126 substance Substances 0.000 claims description 67
- 239000003963 antioxidant agent Substances 0.000 claims description 32
- 230000003078 antioxidant effect Effects 0.000 claims description 32
- 125000000217 alkyl group Chemical group 0.000 claims description 28
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 25
- 229910052698 phosphorus Inorganic materials 0.000 claims description 25
- 239000011574 phosphorus Substances 0.000 claims description 25
- 229910052717 sulfur Inorganic materials 0.000 claims description 21
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 18
- -1 polyethylene Polymers 0.000 claims description 18
- 239000011593 sulfur Substances 0.000 claims description 18
- 150000007942 carboxylates Chemical class 0.000 claims description 17
- 229920000307 polymer substrate Polymers 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 11
- 239000001257 hydrogen Substances 0.000 claims description 11
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 10
- 150000002431 hydrogen Chemical class 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 8
- 125000006671 (C6-C18) aromatic hydrocarbon group Chemical group 0.000 claims description 7
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
- 239000005977 Ethylene Substances 0.000 claims description 6
- 239000004698 Polyethylene Substances 0.000 claims description 6
- 239000004743 Polypropylene Substances 0.000 claims description 6
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
- 229920001577 copolymer Polymers 0.000 claims description 6
- 229920000642 polymer Polymers 0.000 claims description 6
- 150000002430 hydrocarbons Chemical group 0.000 claims description 5
- 229920000573 polyethylene Polymers 0.000 claims description 5
- 229920001155 polypropylene Polymers 0.000 claims description 5
- 239000003381 stabilizer Substances 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000000758 substrate Substances 0.000 claims description 3
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 2
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 238000001125 extrusion Methods 0.000 description 14
- 238000012545 processing Methods 0.000 description 12
- 238000000034 method Methods 0.000 description 9
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 8
- 239000011575 calcium Substances 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 239000011701 zinc Substances 0.000 description 6
- 235000010290 biphenyl Nutrition 0.000 description 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 4
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 4
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- RGASRBUYZODJTG-UHFFFAOYSA-N 1,1-bis(2,4-ditert-butylphenyl)-2,2-bis(hydroxymethyl)propane-1,3-diol dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O.C(C)(C)(C)C1=C(C=CC(=C1)C(C)(C)C)C(O)(C(CO)(CO)CO)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C RGASRBUYZODJTG-UHFFFAOYSA-N 0.000 description 2
- SLJBWNVWFLVATM-UHFFFAOYSA-N C(C)(C)C1=C(C=CC(=C1)C(C)C)C1=C(OP2OCC3(CO2)COP(OC3)OC3=C(C=CC=C3)C3=C(C=C(C=C3)C(C)C)C(C)C)C=CC=C1 Chemical compound C(C)(C)C1=C(C=CC(=C1)C(C)C)C1=C(OP2OCC3(CO2)COP(OC3)OC3=C(C=CC=C3)C3=C(C=C(C=C3)C(C)C)C(C)C)C=CC=C1 SLJBWNVWFLVATM-UHFFFAOYSA-N 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 238000007605 air drying Methods 0.000 description 2
- 229940069428 antacid Drugs 0.000 description 2
- 239000003159 antacid agent Substances 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000010525 oxidative degradation reaction Methods 0.000 description 2
- 238000005453 pelletization Methods 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical compound OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 238000003672 processing method Methods 0.000 description 2
- 238000004383 yellowing Methods 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- GMEVZRPQNQEJHG-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)-1,1-diphenylpropane-1,3-diol Chemical compound C1(=CC=CC=C1)C(O)(C(CO)(CO)CO)C1=CC=CC=C1 GMEVZRPQNQEJHG-UHFFFAOYSA-N 0.000 description 1
- WAOPGHCXGUXHKF-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)-1,1-diphenylpropane-1,3-diol dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O.C1(=CC=CC=C1)C(O)(C(CO)(CO)CO)C1=CC=CC=C1 WAOPGHCXGUXHKF-UHFFFAOYSA-N 0.000 description 1
- BSYJHYLAMMJNRC-UHFFFAOYSA-N 2,4,4-trimethylpentan-2-ol Chemical compound CC(C)(C)CC(C)(C)O BSYJHYLAMMJNRC-UHFFFAOYSA-N 0.000 description 1
- MQWCQFCZUNBTCM-UHFFFAOYSA-N 2-tert-butyl-6-(3-tert-butyl-2-hydroxy-5-methylphenyl)sulfanyl-4-methylphenol Chemical compound CC(C)(C)C1=CC(C)=CC(SC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O MQWCQFCZUNBTCM-UHFFFAOYSA-N 0.000 description 1
- ODJQKYXPKWQWNK-UHFFFAOYSA-L 3-(2-carboxylatoethylsulfanyl)propanoate Chemical compound [O-]C(=O)CCSCCC([O-])=O ODJQKYXPKWQWNK-UHFFFAOYSA-L 0.000 description 1
- DAQUIVMUBOOKRA-UHFFFAOYSA-N 3-tert-butyl-2-(2-tert-butyl-6-hydroxy-3-methylphenyl)sulfanyl-4-methylphenol Chemical compound CC1=CC=C(O)C(SC=2C(=C(C)C=CC=2O)C(C)(C)C)=C1C(C)(C)C DAQUIVMUBOOKRA-UHFFFAOYSA-N 0.000 description 1
- ZIJXMZCTLBEVCJ-UHFFFAOYSA-L C(CCCCCCCCCCC)CC(=S)[O-].[Zn+2].C(CCCCCCCCCCC)CC(=S)[O-] Chemical compound C(CCCCCCCCCCC)CC(=S)[O-].[Zn+2].C(CCCCCCCCCCC)CC(=S)[O-] ZIJXMZCTLBEVCJ-UHFFFAOYSA-L 0.000 description 1
- IPHZKNIGVNVEDL-UHFFFAOYSA-L C(CCCCCCCCCCC)CCC(=S)[O-].[Zn+2].C(CCCCCCCCCCC)CCC(=S)[O-] Chemical compound C(CCCCCCCCCCC)CCC(=S)[O-].[Zn+2].C(CCCCCCCCCCC)CCC(=S)[O-] IPHZKNIGVNVEDL-UHFFFAOYSA-L 0.000 description 1
- GCLSFNUUNXLXKV-UHFFFAOYSA-K C(CCCCCCCCCCCCCCCCC)C(CC(=S)[O-])(CCCCCCCCCCCCCCCCCC)CCCCCCCCCCCCCCCCCC.[Al+3].C(CCCCCCCCCCCCCCCCC)C(CC(=S)[O-])(CCCCCCCCCCCCCCCCCC)CCCCCCCCCCCCCCCCCC.C(CCCCCCCCCCCCCCCCC)C(CC(=S)[O-])(CCCCCCCCCCCCCCCCCC)CCCCCCCCCCCCCCCCCC Chemical compound C(CCCCCCCCCCCCCCCCC)C(CC(=S)[O-])(CCCCCCCCCCCCCCCCCC)CCCCCCCCCCCCCCCCCC.[Al+3].C(CCCCCCCCCCCCCCCCC)C(CC(=S)[O-])(CCCCCCCCCCCCCCCCCC)CCCCCCCCCCCCCCCCCC.C(CCCCCCCCCCCCCCCCC)C(CC(=S)[O-])(CCCCCCCCCCCCCCCCCC)CCCCCCCCCCCCCCCCCC GCLSFNUUNXLXKV-UHFFFAOYSA-K 0.000 description 1
- BMIWADQNWYTVLW-UHFFFAOYSA-N C1(=CC=CC=C1)P(C1=CC=CC=C1)C1=CC=CC=C1.C1(=CC=CC=C1)OP(OC1=CC=CC=C1)OC1=CC=CC=C1 Chemical compound C1(=CC=CC=C1)P(C1=CC=CC=C1)C1=CC=CC=C1.C1(=CC=CC=C1)OP(OC1=CC=CC=C1)OC1=CC=CC=C1 BMIWADQNWYTVLW-UHFFFAOYSA-N 0.000 description 1
- ZSVIEHBJSABTNJ-UHFFFAOYSA-N CC(C)(C)C1=CC(=C(C=C1)C2=CC(=C(C(=C2C(C)(C)C)C3=C(C=C(C=C3)C(C)(C)C)C(C)(C)C)C(C)(C)C)P(C)(O)(O)O)C(C)(C)C Chemical compound CC(C)(C)C1=CC(=C(C=C1)C2=CC(=C(C(=C2C(C)(C)C)C3=C(C=C(C=C3)C(C)(C)C)C(C)(C)C)C(C)(C)C)P(C)(O)(O)O)C(C)(C)C ZSVIEHBJSABTNJ-UHFFFAOYSA-N 0.000 description 1
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical class [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 241000285023 Formosa Species 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000001458 anti-acid effect Effects 0.000 description 1
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 1
- DWSWCPPGLRSPIT-UHFFFAOYSA-N benzo[c][2,1]benzoxaphosphinin-6-ium 6-oxide Chemical compound C1=CC=C2[P+](=O)OC3=CC=CC=C3C2=C1 DWSWCPPGLRSPIT-UHFFFAOYSA-N 0.000 description 1
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 1
- PPDHTJBSTYCATN-UHFFFAOYSA-L calcium pentadecanethioate Chemical compound C(CCCCCCCCCCC)CCC(=S)[O-].[Ca+2].C(CCCCCCCCCCC)CCC(=S)[O-] PPDHTJBSTYCATN-UHFFFAOYSA-L 0.000 description 1
- DNXAROCMSIHFQJ-UHFFFAOYSA-L calcium tetradecanethioate Chemical compound C(CCCCCCCCCCC)CC(=S)[O-].[Ca+2].C(CCCCCCCCCCC)CC(=S)[O-] DNXAROCMSIHFQJ-UHFFFAOYSA-L 0.000 description 1
- DSSYKIVIOFKYAU-UHFFFAOYSA-N camphor Chemical compound C1CC2(C)C(=O)CC1C2(C)C DSSYKIVIOFKYAU-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- PWWSSIYVTQUJQQ-UHFFFAOYSA-N distearyl thiodipropionate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCCCCCC PWWSSIYVTQUJQQ-UHFFFAOYSA-N 0.000 description 1
- 229940000406 drug candidate Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000003777 experimental drug Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- JKBYAWVSVVSRIX-UHFFFAOYSA-N octadecyl 2-(1-octadecoxy-1-oxopropan-2-yl)sulfanylpropanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)SC(C)C(=O)OCCCCCCCCCCCCCCCCCC JKBYAWVSVVSRIX-UHFFFAOYSA-N 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- VCAFTIGPOYBOIC-UHFFFAOYSA-N phenyl dihydrogen phosphite Chemical compound OP(O)OC1=CC=CC=C1 VCAFTIGPOYBOIC-UHFFFAOYSA-N 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000006076 specific stabilizer Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 1
- SAAMKFBWYWFBNY-UHFFFAOYSA-N tris(4-tert-butylphenyl) phosphite Chemical compound C1=CC(C(C)(C)C)=CC=C1OP(OC=1C=CC(=CC=1)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1 SAAMKFBWYWFBNY-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K15/00—Anti-oxidant compositions; Compositions inhibiting chemical change
- C09K15/04—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds
- C09K15/32—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing two or more of boron, silicon, phosphorus, selenium, tellurium or a metal
- C09K15/322—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing two or more of boron, silicon, phosphorus, selenium, tellurium or a metal containing only phosphorus
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F236/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F236/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F236/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
- C08F236/14—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated containing elements other than carbon and hydrogen
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/13—Phenols; Phenolates
- C08K5/134—Phenols containing ester groups
- C08K5/1345—Carboxylic esters of phenolcarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/005—Stabilisers against oxidation, heat, light, ozone
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/13—Phenols; Phenolates
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C08K5/1535—Five-membered rings
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/22—Compounds containing nitrogen bound to another nitrogen atom
- C08K5/24—Derivatives of hydrazine
- C08K5/25—Carboxylic acid hydrazides
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/37—Thiols
- C08K5/372—Sulfides, e.g. R-(S)x-R'
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- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/37—Thiols
- C08K5/378—Thiols containing heterocyclic rings
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/38—Thiocarbonic acids; Derivatives thereof, e.g. xanthates ; i.e. compounds containing -X-C(=X)- groups, X being oxygen or sulfur, at least one X being sulfur
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
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Description
本發明是有關於一種經改質的聚合物材料,特別是指一種透過一包括特定的含磷有機抗氧化劑及含硫羧酸鹽化合物的複合式安定劑組成物將烯烴系聚合物或乙烯/醋酸乙烯酯共聚物改質之經改質的聚合物材料。
聚合物基材,例如烯烴系聚合物、乙烯/醋酸乙烯酯共聚物具有良好的化學穩定性、機械強度、電氣絕緣性及製品尺寸安定性,並具有無毒性且易於加工等優點,因而被廣泛應用作為各種產品。聚合物基材雖具有上述優點,但上述聚合物基材在熱能作用下容易被氧化降解,造成黃變以及機械性質下降。
因此,為了防止上述聚合物基材的氧化降解,可在加工成型製程中加入抗氧化劑來降低聚合物基材的氧化降解作用,以增強聚合物基材的機械性質及耐熱性;然而,抗氧化劑本身可能導致聚合物基材帶色及加工穩定性下降。此外,一般在加工成型製程中會再加入制酸劑,是為了抑制酸性物質造成聚合物基材降解,然
而,某些制酸劑的種類或者添加量較多時,也會導致聚合物基材帶色及加工穩定性下降。
因此,本發明之第一目的,即在提供一種經改質的聚合物材料,其在加工成型製程中,能夠維持較佳的顏色穩定性及加工穩定性。
於是,本發明經改質的聚合物材料包含:一聚合物基材,是選自於烯烴系聚合物、乙烯/醋酸乙烯酯共聚物或上述之組合;及一複合式安定劑組成物,包括:一種選自於化學式1至化學式8中至少一者的含磷有機抗氧化劑,及一種選自於化學式9至化學式12中至少一者所示的含硫羧酸鹽,
【化學式7】
在化學式1至化學式7中,R11至R13、R21至R26、R31至R35、R41至R48、R51至R56、R61至R64,及R71至R78各自獨立地表示氫、第三丁基、異丙苯基或C1至C8直鏈烷基;T
表示C1至C18烴基或,R65至R67各自獨立地表
示氫、第三丁基、異丙苯基或C1至C8直鏈烷基;Z41、Z42、Z51及Z61各自獨立地表示O、S或C1至C4伸烷基,
在化學式9中,Mq+表示Ca2+、Mg2+、Ba2+、Zn2+或Al3+,q表示2或3,t表示0至6的整數,R91表示氫或C1至C18烷基,R92表示C1至C30烷基、C6至C18芳烴基或R93OOC-(CH2)k-,其中,R93表示C1至C30烷基或C6至C18芳烴基,k表示1至5的整數,
化學式10中,X11及X12各自獨立地表示Ca2+、Ba2+、Mg2+或Zn2+,Y11及Y12各自獨立地表示C1至C30烷基或C6至C18芳烴基,a及b各自獨立地表示1至6,
化學式11中,p表示1至9的整數,X21表示Ca2+、Ba2+、Mg2+或Zn2+,G1及G2各自獨立地表示
,其中,c及d各自獨立地表示1
至6,且當p2時,多個G1可為相同或不同,多個X21可為相同或不同,
在化學式12中,X31表示Ca2+、Ba2+、Mg2+、Zn2+,Y31表示C1至C30烷基、C6至C18芳烴基或R93OOC-(CH2)k-,其中,R93表示C1至C30烷基或C6至C18芳烴基,k表示1至5的整數。
因此,本發明之第二目的,即在提供一種複合式安定劑組成物,是用於改質上述的聚合物基材。
於是本發明複合式安定劑組成物包含:一種選自於化學式1至化學式8中至少一者的含磷有機抗氧化劑,以及一種選自於化學式9至化學式12中至少一者所示的含硫羧酸鹽。其中,該化學式1至12是如上所述,故不再贅述。
本發明之功效在於:透過在該聚合物基材中添加含有特定的含磷有機抗氧化劑及含硫羧酸鹽的該複合式安定劑組成物,使得該經改質的聚合物材料在加工製程中能維持良好的顏色穩定性及加工穩定性,繼而製得高品質的成型品。
以下將就本發明內容進行詳細說明:[聚合物基材]
該聚合物基材是選自於烯烴系聚合物、乙烯/醋酸乙烯酯共聚物或上述之組合。較佳地,該烯烴系聚合物是選自於聚乙烯、聚丙烯或上述的一組合。
[複合式安定劑組成物]
該化學式1所示的含磷有機抗氧化劑例如但不限於:三(2,4-二第三丁基)亞磷酸苯酯[tris(2,4-ditert-butylphenyl)phosphite,簡稱抗氧化劑168]、亞磷酸三苯酯(triphenyl
phosphite)、三(4-第三丁基苯基)亞磷酸酯[tris(4-tert-butylphenyl)phosphite]、三(壬基苯基)亞磷酸酯[tris(nonylphenyl)phosphite],或三(對-異丙苯基苯基)亞磷酸酯[tris(p-cumylphenyl)phosphite]。
該化學式2所示的含磷有機抗氧化劑例如但不限於:雙(2,4-二第三丁基苯基)季戊四醇二亞磷酸酯(簡稱抗氧化劑626)、3,9-雙(2,4-二異丙苯基苯氧基)-2,4,8,10-四氧雜-3,9-二磷雜螺[5.5]十一烷(簡稱抗氧化劑9228)、二苯基季戊四醇二亞磷酸酯(diphenyl pentaerythritol diphosphite),或2,4,8,10-四氧雜-3,9-二磷雜螺[5.5]十一烷{2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane}。
該化學式3所示的含磷有機抗氧化劑例如但不限於:
(CAS號碼為161717-32-4)、2-[2,4-雙
(1,1-二甲基乙基)苯氧基]-5,5-二甲基-1,3,2-二氧磷雜環己烷{2-[2,4-bis(1,1-dimethylethyl)phenoxy]-5,5-dimethyl-1,3,2-dioxaphosphorinane}、2,4-二異丙苯基苯基-2-丁基-2-乙基-1,3-丙二醇亞磷酸酯(2,4-dicumylphenyl 2-butyl-2-ethyl-1,3-propanediol phosphite)、2-[2,4-雙(1,1-
二甲基乙基)苯氧基]-5-丁基-5-乙基-1,3,2-二氧磷雜環己烷{2-[2,4-bis(1,1-dimethylethyl)phenoxy]-5-butyl-5-ethyl-1,3,2-dioxaphosphorinane}。
該化學式4所示的含磷有機抗氧化劑例如但不限於:
(CAS號碼為
1601458-04-1)。
該化學式5所示的含磷有機抗氧化劑例如但不限於:
(CAS號碼為205518-79-2)。
該化學式6所示的含磷有機抗氧化劑例如但不限於:2,4,8,10-四第三丁基-6-[(2-乙己基)氧]-12H-二苯基[d,g][1,3,2]二氧磷雜八環(簡稱HP-10)、2,2'-硫代二[第三丁基-對甲酚]環狀單苯基亞磷酸酯{2,2'-thiobis[6-tert-butyl-p-cresol]cyclic monophenyl
phosphite}、2,2'-伸甲基雙(4,6-二第三丁基苯基)(2,4-二第三丁基苯基)亞磷酸酯[2,2'-methylene bis(4,6-di-tert-butylphenyl)(2,4-di-tert-butylphenyl)phosphite]。
化學式7所示的含磷有機抗氧化劑例如但不限於:抗氧化劑P-EPQ、膦酸[1,1'-聯苯]-4,4'-二基雙-四[2-(1,1-二甲基乙基)苯基]酯{phosphonous acid,[1,1'-biphenyl]-4,4'-diylbis-,tetrakis[2-(1,1-dimethyl ethyl)phenyl]ester}、膦酸[1,1'-聯苯]-4,4'-二基雙-三苯基酯{phosphonous acid,[1,1'-biphenyl]-4,4'-diylbis-,tetraphenyl ester}。
較佳地,該化學式9中的R91表示氫,R92表示C1至C18烷基、C6至C18芳烴基或R93OOC-(CH2)k-,其中,R93表示C1至C18烷基,k表示1或2。上述的芳烴基指的是芳基、烴基取代的芳基或芳基取代的烴基。更佳地,該化學式9中的R92表示十二烷基或H17C8OOCCH2-。該化學式9所示的含硫羧酸鹽例如但不限於:2-十二烷基硫基乙酸鋅、2-十二烷基硫基乙酸鈣、3-十二烷基硫基丙酸鋅、3-十二烷基硫基丙酸鈣或3-十八烷基硫基丙酸鋁。
較佳地,該化學式10中,X11及X12各自獨立地表示Ca或Zn,Y11及Y12各自獨立地表示-C7H15或-C17H35。該化學式10所示的含硫羧酸鹽例如但不限於:
較佳地,該化學式11中,X21表示Ca或Zn,G1及G2
各自獨立地表示,其中c及d各自獨立地
表示1或2。該化學式11所示的含硫羧酸鹽例如但不限於:
,其中,p表示1
至9的整數。
該化學式12所示的含硫羧酸鹽例如但不限於:
該含磷有機抗氧化劑與該含硫羧酸鹽的用量比例範圍為1:99至99:1。
[經改質的聚合物材料]
較佳地,以該聚合物基材的重量為100重量份,該複合式安定劑組成物的含量範圍為0.01至2.2重量份。
該經改質的聚合物材料的製備方法並無特別限制,例如但不限於將該聚合物基材與該複合式安定劑組成物混合即可。
該經改質的聚合物材料的加工成型方式並無特別限制,可依據後續的產品需求,採用烯烴系聚合物、乙烯/醋酸乙烯酯共聚物常用的加工成型方式即可。該加工成型的方式例如但不限於押出成型、射出成型等。
本發明將就以下實施例來作進一步說明,但應瞭解的是,該實施例僅為例示說明之用,而不應被解釋為本發明實施之限制。
[實驗藥品]
1.聚丙烯:購自於台化公司,品名為B8001,表1及表2中簡稱
PP。
2.聚乙烯:購自於台塑公司,品名為LL120,表1及表2中簡稱PE。
3.三(2,4-二第三丁基)亞磷酸苯酯:為化學式1所示的含磷有機抗氧化劑,簡稱抗氧化劑168,表1及表2中簡稱A1。
4.雙(2,4-二第三丁基苯基)季戊四醇二亞磷酸酯:為化學式2所示的含磷有機抗氧化劑,簡稱抗氧化劑626,表1及表2中簡稱A2。
5. 3,9-雙(2,4-二異丙苯基苯氧基)-2,4,8,10-四氧雜-3,9-二磷雜螺[5.5]十一烷:為化學式2所示的含磷有機抗氧化劑,簡稱抗氧化劑9228,表1及表2中簡稱A3。
6. 2,4,8,10-四第三丁基-6-[(2-乙己基)氧]-12H-二苯基[d,g][1,3,2]二氧磷雜八環:為化學式6所示的含磷有機抗氧化劑,簡稱HP-10,表1及表2中簡稱A4。
7.:為化學
式7所示的含磷有機抗氧化劑,簡稱P-EPQ,表1及表2中簡稱A5。
8. 9,10-二氫-9-氧雜-10-磷雜菲-10-氧化物:為化學式8所示的含磷有機抗氧化劑,簡稱DOPO,表1及表2中簡稱A6。
9.:為化學式3所示的含磷有機抗氧
化劑,CAS號碼為161717-32-4,表1及表2中簡稱A7。
10.:為化學式5所示的含磷有機抗
氧化劑,CAS號碼為205518-79-2,表1及表2中簡稱A8。
11.:為化學式4
所示的含磷有機抗氧化劑,CAS號碼為1601458-04-1,表1及表2中簡稱A9。
12.[C12H25-S-CH2CH2COO]2Ca:為化學式9所示的含硫羧酸鹽,表1及表2中簡稱B1。
13.[C12H25-S-CH2CH2COO]3Al:為化學式9所示的含硫羧酸鹽,表1及表2中簡稱B2。
14.:為化
學式10所示的含硫羧酸鹽,表1及表2中簡稱B3;
15.
為化學式11所示的含硫羧酸鹽,表1及表2中簡稱B4。
16.:為化學式12所示的含硫羧酸鹽,表1及
表2中簡稱B5。
17.硫代二丙酸雙十八酯:英文名為disteaxyl thiodipropionate,以下簡稱DSTDP。
<實施例1至17>經改質的聚合物材料
依據表1所示的組成成分及比例(重量份),將100重量份聚丙烯或100重量份聚乙烯與複合式安定劑組成物在25℃下均勻混合,分別得到實施例1至17的經改質的聚合物材料E1'至E17'。
<比較例1至21>經改質的聚合物材料
依據表2所示的組成成分及比例(重量份),將100重量份聚丙烯或100重量份聚乙烯與安定劑組成物在25℃下均勻混合,分別得到比較例1至21的經改質的聚合物材料CE1'至CE21'。
[評價測試]
將上述經改質的聚合物材料E1'至E17'以及CE1'至CE21'分別以雙螺桿押出機(台灣弘煜機械公司試驗機PSM20A)混合押出(溫度設定為190至230℃,螺桿轉速為200轉/分鐘,進料速度為6轉/分鐘),再經過冷卻、風乾、切粒、乾燥,製備出樣品E1至E17及CE1至CE21。將樣品E1至E17及CE1至CE21分別重複進行上述押出、冷卻、風乾、切粒、乾燥步驟,以評估樣品在經過多次加工成型的程序後黃色度及熔融指數的變化,黃色度的變化越小代表經改質的聚合物材料在加工成型製程中的顏色穩定性越
佳,熔融指數的變化越小代表經改質的聚合物材料在加工成型製程中的加工穩定性越佳。
1.黃色色差(△b*值)
使用色差儀(為HunterLab公司的ColorQuest XE)分別測量樣品E1至E17及CE1至CE21在第3次及第5次押出後相較於第1次押出的色差值(△b*值),結果如表3及表4所示。
2.熔融指數(melting index,MI)變化(△MI)
使用實驗室熔融指數儀(為Dynisco公司的Laboratory Melt Indexer LMI D4004)分別測量樣品E1至E17及CE1至CE21在第3次及第5次押出後相較於第1次押出的熔融指
,結果如表3及表4所示。
由表3及表4可以得知,由實施例1至17製得的樣品E1至E17,經第3次押出的△b*值在2.66以下,經第5次押出的△b*值在5.04以下,然而,由比較例1至21製得的樣品CE1至CE21,經第3次押出的△b*值在3.12以上,經第5次押出的△b*值在6.12以上,顯示相較於比較例1至21使用安定劑組成物,實施例1至17經改質的聚合物材料透過使用該複合式安定劑組成物,使得經改質
的聚合物材料具有較佳的顏色穩定性,進而使得所製得的樣品具有較低的黃色色差(△b*值),黃變較不明顯。
根據熔融指數變化(△MI)的結果,由實施例1至17製得的樣品E1至E17,經第3次押出的△MI在161.58%以下,經第5次押出的△MI在258.64%以下;然,由比較例1至21製得的樣品CE1至CE21,經第3次押出的△MI在175.79%以上,經第5次押出的△MI在314.41%以上,顯示相較於比較例1至21使用安定劑組成物,實施例1至17經改質的聚合物材料透過使用該複合式安定劑組成物,使得經改質的聚合物材料具有較佳的加工穩定性(物性),進而使得所製得的樣品具有較低的熔融指數變化(△MI)。
綜上所述,本發明透過在該聚合物基材中添加含有特定的含磷有機抗氧化劑及該含硫羧酸鹽的該複合式安定劑組成物,使得該經改質的聚合物材料在加工製程中能維持良好的顏色穩定性及加工穩定性,故確實能達成本發明之目的。
惟以上所述者,僅為本發明之實施例而已,當不能以此限定本發明實施之範圍,凡是依本發明申請專利範圍及專利說明書內容所作之簡單的等效變化與修飾,皆仍屬本發明專利涵蓋之範圍內。
Claims (6)
- 一種經改質的聚合物材料,包含:一聚合物基材,是選自於烯烴系聚合物、乙烯/醋酸乙烯酯共聚物或上述之組合;及一複合式安定劑組成物,包括:一種選自於化學式1至化學式8中至少一者的含磷有機抗氧化劑,及一種選自於化學式9至化學式12中至少一者的含硫羧酸鹽,
- 如請求項1所述的經改質的聚合物材料,其中,以該聚合物基材的重量為100重量份,該複合式安定劑組成物的含量範圍為0.01至2.2重量份。
- 如請求項1所述的經改質的聚合物材料,其中,該烯烴系聚合物是選自於聚乙烯、聚丙烯或上述的一組合。
- 一種複合式安定劑組成物,包括:一種選自於化學式1至化學式8中至少一者的含磷有機抗氧化劑;及一種選自於化學式9至化學式12中至少一者的含硫羧酸鹽;但不包括化學式1含磷有機抗氧化劑及化學式9含硫羧酸鹽的組合;
- 如請求項4所述的複合式安定劑組成物,其中,該化學式9中的R91表示氫,R92表示C1至C18烷基、C6至C18芳烴基或R93OOC-(CH2)k-,其中,R93表示C1至C18烷基,k表示1或2。
- 如請求項5所述的複合式安定劑組成物,其中,該化學式9中的R92表示十二烷基或H17C8OOCCH2-。
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